Completed

Central Motor Physiology in Polio Survivors

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What is being collected

Data Collection

Who is being recruted

Neuroinflammatory Diseases
+10

+ Central Nervous System Diseases
+ Central Nervous System Infections
From 21 to 80 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: April 2004
See protocol details

Summary

Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: April 6, 2004Actual date on which the first participant was enrolled.

OBJECTIVE: Many persons who survive poliomyelitis develop pain, weakness, and fatigue many decades later. It is not known why some persons develop this syndrome and others do not. One possibility is that polio caused subclinical damage to the motor cortex. Autopsies in some polio patients have found damage to the brainstem and motor cortex as well as to spinal motor neurons. Alternatively, polio may have spared the motor cortex, but the cortex reorganized in different ways to compensate for the loss of spinal motor neurons. This study will first assess the integrity of central motor pathways in polio survivors with and without postpolio syndrome. The second goal will be to investigate differences in the intracortical mechanisms for controlling muscles affected and unaffected by polio. STUDY POPULATION: 60 patients who survived polio in childhood. Only patients with an unequivocal history of polio will be referred to this study. Half of the patients will have the post-polio syndrome. 30 normal volunteers, aged 21-80. DESIGN: Patients will be screened at the collaborating institution, the Uniformed Services University of the Health Sciences, which will also perform sensory evoked potential testing. At NIH, motor evoked potentials will be elicited from all four limbs using transcranial magnetic stimulation to assess central motor conduction time and threshold. MRI scans of the brain or spine will be performed in patients with abnormal evoked potentials. Intracortical facilitation will be assessed using paired-pulse magnetic stimulation. Two muscles will be tested in each patient, one affected by polio and one unaffected by polio. In the affected muscle, intracortical facilitation will be assessed again after exercises it until it fatigues. OUTCOME PARAMETERS: Cortical thresholds and central motor conduction times to all four limbs will be measured in patients and compared to normal subjects. The mean intracortical facilitation at rest will be compared in affected and unaffected muscles in polio patients with and without post-polio syndrome.

Official TitleCentral Motor Physiology in Polio Survivors 
NCT00080600
Principal SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Last updated: January 14, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details
90 patients to be enrolledTotal number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria
Any sexBiological sex of participants that are eligible to enroll.
From 21 to 80 YearsRange of ages for which participants are eligible to join.
Healthy volunteers allowedIf individuals who are healthy and do not have the condition being studied can participate.
Conditions
Pathology
Neuroinflammatory Diseases
Central Nervous System Diseases
Central Nervous System Infections
Enterovirus Infections
Infections
Myelitis
Nervous System Diseases
Neuromuscular Diseases
Picornaviridae Infections
Poliomyelitis
RNA Virus Infections
Spinal Cord Diseases
Virus Diseases
Criteria

* INCLUSION CRITERIA: POLIO PATIENTS: Complete screening evaluation. Meet clinical criteria for diagnosis of past polio (see below). Meet clinical criteria for the diagnosis of PPS (PPS group only) and have new muscle weakness. Age 21 or older. CLINICAL CRITERIA FOR PAST POLIO (CONFIRMED): Clinically compatible signs and symptoms of paralytic poliomyelitis (acute flaccid paralysis of one or more limbs). Decreased or absent tendon reflexes on the affected limbs. No persistent sensory or cognitive loss. No other apparent cause (including laboratory investigation to rule out other causes of similar syndrome). Neurological deficit present 60 days after onset of initial symptoms. Associated with isolation of either vaccine or wild poliovirus from a clinical specimen. CLINICAL CRITERIA FOR POST-POLIO SYNDROME: History of polio with partial or complete neurological and functional recovery. Stable function greater than 15 years. New onset of one or more of the following: fatigue, weakness, atrophy, muscle pain, functional loss. Exclusion of other explanations for the symptomatology. Neurological evaluation demonstrating: lower motor neuron dysfunction (confirmed by EMG, imaging studies or muscle biopsy), no sensory loss. Must have new onset of muscle weakness in one or more limb muscles, as determined by history and clinical examination. NORMAL VOLUNTEERS: Healthy adult volunteers ages 21-80 who are willing to participate. EXCLUSION CRITERIA: Neurological diseases or conditions, other than polio, that in the judgment of the investigators may account for the symptoms or interfere with the experimental interventions. Implanted devices, such as pumps, pacemakers, or metal fragments in the skull or eye.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has 2 locations
Suspended
Uniformed Services University of the Health SciencesBethesda, United StatesSee the location
Suspended
National Institutes of Health Clinical Center, 9000 Rockville PikeBethesda, United States
Completed2 Study Centers